enalapril maleate

Generic: enalapril maleate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 20 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4153
Product ID 70518-4153_3fb64f07-84a0-ce6c-e063-6394a90ac91b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075479
Listing Expiration 2026-12-31
Marketing Start 2024-08-01

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa] decreased blood pressure [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184153
Hyphenated Format 70518-4153

Supplemental Identifiers

RxCUI
858810
UNII
9O25354EPJ

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name enalapril maleate (source: ndc)
Generic Name enalapril maleate (source: ndc)
Application Number ANDA075479 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-4153-0)
  • 100 TABLET in 1 BOTTLE, PLASTIC (70518-4153-1)
source: ndc

Packages (2)

Ingredients (1)

enalapril maleate (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fb64f07-84a0-ce6c-e063-6394a90ac91b", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["7077d32e-4b06-4d48-ba0c-6db2f8ebe08c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4153-0)", "package_ndc": "70518-4153-0", "marketing_start_date": "20240801"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-4153-1)", "package_ndc": "70518-4153-1", "marketing_start_date": "20250320"}], "brand_name": "Enalapril maleate", "product_id": "70518-4153_3fb64f07-84a0-ce6c-e063-6394a90ac91b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-4153", "generic_name": "Enalapril maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075479", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}